A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191092



Internal ID20758132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32499801..32509100hg38UCSC Ensembl
chr9:32499799..32509098hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439495
Supporting Variants
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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